Canonical Allele Identifier: CA849557684
Gene: LPL HGNC NCBI

Linked Data

dbSNP Id: rs1226917616
MyVariant Identifiers: chr8:g.19809683T>C (hg19) chr8:g.19952172T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19952172T>C , CM000670.2:g.19952172T>C GRCh38
NC_000008.10:g.19809683T>C , CM000670.1:g.19809683T>C GRCh37
NC_000008.9:g.19853963T>C NCBI36
NG_008855.1:g.18102T>C
NG_008855.2:g.55456T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000650287.1:c.429+224T>C MANE Select ENSP00000497642.1:n.429+224T>C
ENST00000311322.8:c.429+224T>C ENSP00000309757.6:n.429+224T>C
ENST00000520959.5:c.201+224T>C ENSP00000428496.1:n.201+224T>C
NM_000237.2:c.429+224T>C NP_000228.1:n.429+224T>C
NM_000237.3:c.429+224T>C MANE Select NP_000228.1:n.429+224T>C
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